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NOT YET RECRUITING
NCT06620393
PHASE2/PHASE3

Effects of Dexmedetomidine on Agitation in Critically Ill TBI Patients

Sponsor: Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal

View on ClinicalTrials.gov

Summary

Agitation is a frequent complication following traumatic braing injury in patients admitted to the intensive care unit. This agitation frequently results in the liberal use of rescue drugs such as antipsychotics, sedatives and opiates, which in turn may delay rehabilitation, liberation from mechanical ventilation and emergence from posttraumatic amnesia. Dexmedetomidine may be a better agent given it's light sedative properties. The main objective is to assess the feasibility of conducting a multicenter randomized controlled trial of dexmedetomidine following TBI in the ICU.

Official title: Effects of Dexmedetomidine on Agitation in Critically Ill TBI Patients (DEX-TBI)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

72

Start Date

2024-10-01

Completion Date

2026-12-01

Last Updated

2024-10-01

Healthy Volunteers

No

Interventions

DRUG

Dexmedetomidine

DEX 4 mcg/100 ml at a starting dose of 0.6 mcg/kg/hour and increased by 0.2 mcg/kg/hour every 30 minutes up to final dose of 1.4 mcg/kg/hour.

DRUG

Placebo

NaCl 0.9% 100ml